HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429846C>G , CM000663.2:g.68429846C>G | GRCh38 |
NC_000001.10:g.68895529C>G , CM000663.1:g.68895529C>G | GRCh37 |
NC_000001.9:g.68668117C>G | NCBI36 |
NG_008472.1:g.25114G>C | |
NG_008472.2:g.25114G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1532G>C MANE Select | ENSP00000262340.5:p.Ser511Thr | |
ENST00000262340.5:c.1532G>C | ENSP00000262340.5:p.Ser511Thr | |
NM_000329.2:c.1532G>C | NP_000320.1:p.Ser511Thr | |
XM_017002027.1:c.1256G>C | XP_016857516.1:p.Ser419Thr | |
NM_000329.3:c.1532G>C MANE Select | NP_000320.1:p.Ser511Thr |